ZipRecruiter

Log In

2

Remote Medical Device Engineer Jobs in Oregon (NOW HIRING)

Stryker

Senior Staff Medical Writer (Remote)

Portland, OR · On-site +1

$143K - $238K/yr

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745 ...

AcuityMD

Enterprise Account Executive

OR · On-site +1

$240K - $300K/yr

You have 5+ years of experience selling Enterprise SaaS or Medical Device products * You should ... Remote work : AcuityMD is committed to supporting full-remote flexibility for employees in the US.

AcuityMD

Strategic Account Executive

OR · On-site +1

You have 5+ years of experience selling Enterprise SaaS or Medical Device products * You should ... Remote work : AcuityMD is committed to supporting full-remote flexibility for employees in the US.

Fortive

Field Service Engineer

Portland, OR · On-site +1

Portalnd, Oregon - with 75% overnight travel Under remote supervision, Advanced Sterilization ... Preferred Qualifications: * 4+ years of work experience in a related Medical Device industry.

ZEISS

Global Technical Escalation Engineer

OR · On-site +1

... medical device industry. * High degree of technical proficiency, excellent structured problem ... Experience with remote support systems. * Excellent communication and interpersonal skills.

A-dec, Inc.

Quality Assurance Specialist, Sr

Newberg, OR · Remote

$86K - $119K/yr

... Medical Device regulations and standards including US-FDA, Health Canada, and the European Union ... Fully remote is not an option due to manufacturing facility-based activities. Education and ...

Varsity Tutors

Biomedical Engineering Tutor

OR · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Varsity Tutors

Biomedical Engineering Tutor

Eugene, OR · Remote

$18 - $40/hr

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

Bausch + Lomb

Product Cybersecurity Architect

OR · On-site +1

Partner with engineering teams to implement security testing practices, including SAST, DAST, SCA ... Demonstrated experience supporting or leading cybersecurity activities for medical device or other ...

AcuityMD

Growth Account Executive

OR · On-site +1

$150K - $200K/yr

... Medical Device Industry. Our Commercial Team takes a proactive, consultative, and high-touch ... Remote work : AcuityMD is committed to supporting full-remote flexibility for employees in the US.

next page

Showing results 1-20

All JobsMedical Device Engineer JobsRemote Medical Device Engineer JobsRemote Medical Device Engineer Jobs in Oregon

Remote Medical Device Engineer information

See Oregon salary details

$22

$52

$102

How much do remote medical device engineer jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for remote medical device engineer in Oregon is $52.69, according to ZipRecruiter salary data. Most workers in this role earn between $37.12 and $63.03 per hour, depending on experience, location, and employer.

What is a remote medical device engineer?

A Remote Medical Device Engineer designs, develops, and tests medical devices while working from a remote location. They ensure compliance with industry regulations and collaborate with cross-functional teams to improve device functionality and safety. Responsibilities may include CAD modeling, prototyping, software integration, and regulatory documentation. Remote engineers use digital tools to communicate with teams and manage development processes efficiently. Strong technical expertise and knowledge of medical device regulations are essential for this role.

What is a typical workday like for a remote medical device engineer?

A typical workday as a Remote Medical Device Engineer often involves designing and reviewing device components using CAD software, participating in virtual meetings to coordinate with R&D, quality assurance, and regulatory teams, and conducting documentation for regulatory submissions. You may also troubleshoot technical issues, analyze test data, and provide design updates based on feedback or test results. Regular communication with colleagues across different time zones is common, requiring flexibility and excellent organizational skills. The remote nature of the role typically offers autonomy and flexibility while maintaining close collaboration with diverse, cross-functional teams to ensure projects progress smoothly.

What are the key skills and qualifications needed to thrive as a remote medical device engineer?

To thrive as a Remote Medical Device Engineer, you need a solid background in biomedical engineering or related fields, along with experience in product development, regulatory compliance, and device testing. Familiarity with CAD software, FDA regulations (such as 21 CFR Part 820), and risk management systems is typically required, and certifications like PMP or Six Sigma can be advantageous. Strong problem-solving abilities, effective remote communication skills, and the ability to collaborate across distributed teams are crucial soft skills. These qualifications ensure that engineers can design safe, compliant devices and contribute effectively to remote, cross-functional teams.

What are popular job titles related to Remote Medical Device Engineer jobs in Oregon?

For Remote Medical Device Engineer jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Remote Medical Device Engineer jobs in Oregon look for?

The top searched job categories for Remote Medical Device Engineer jobs in Oregon are:

What cities in Oregon are hiring for Remote Medical Device Engineer jobs?

Cities in Oregon with the most Remote Medical Device Engineer job openings:

Remote Medical Device Engineer jobs near you

Associate Director, Device Engineering

Kailera Therapeutics, Inc.

OR • On-site, Remote

Full-time

Posted 4 days ago

Job description

What You'll Do:

We are seeking an experienced Associate Director, Device Engineering, to lead the development and launch of drug-device combination products, with a strong emphasis on autoinjectors, pre-filled syringes, and multidose pens. This role will drive cross-functional collaboration across CMC, quality, regulatory, manufacturing, clinical, and commercial teams to ensure robust product development aligned with meeting patient needs, global standards, and regulatory expectations.

Required location: Waltham, MA (hub-based, onsite 3-4 days per week) OR Remote (home-based, onsite at a hub 1 week every other month).

Responsibilities:

  • Lead combination product development projects (prefilled syringes, autoinjectors, and/or multidose pens) from concept through commercialization
  • Build and execute project plans with clearly defined risks and milestones
  • Develop device and combination product requirements, including user and stakeholder needs and technical requirements, and ensure appropriate engineering translation and subsequent verification and validation of requirements
  • Oversee and ensure compliance with design controls per FDA and ISO 13485 requirements
  • Manage risk management activities in accordance with ISO 14971, including hazard analysis, FMEA, and risk mitigation strategies
  • Drive design verification and validation activities, including test method development, protocol execution, and documentation
  • Oversee human factors and usability engineering efforts, ensuring compliance with FDA guidance and IEC 62366
  • Facilitate design transfer to manufacturing, ensuring smooth transition and scalability
  • Partner cross-functionally with CMC, quality, regulatory, clinical development, commercial/marketing, supply chain, and other key functions to ensure critical inputs are integrated into device development activities
  • Author relevant portions of regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for devices and combination product programs
  • Manage and collaborate with vendors, including Contract Design and Manufacturing Organizations (CDMOs) and suppliers, to ensure components and products meet quality and technical requirements and to integrate deliverables into the project Design History File at various stages of development and manufacturing
  • Manage and collaborate with contract test labs to ensure testing strategy, method validation, and test execution are aligned with relevant standards and quality and technical requirements and integrate testing results into the Design History File
  • Ensure product development aligns with relevant standards including ISO 11608-1, ISO 11040, ASTM D4169, ISO 14971, IEC 62366

Required Qualifications:

  • Minimum of 10+ years of experience in medical device or combination product development, with at least 3 years in a team leadership role
  • Proven experience with autoinjector, pre-filled syringe, or multidose pen development and launch, including authoring clinical and commercial regulatory submissions
  • Deep understanding of design controls, design verification, test method development and validation, risk management, human factors, and design transfer
  • Strong knowledge of applicable regulatory standards and guidance documents
  • Excellent communication, leadership, and cross-functional collaboration skills

 

Preferred Qualifications:

  • Experience working in a regulated pharmaceutical or biotech environment
  • Familiarity with combination product regulations (21 CFR Part 4)
  • Experience with supplier management of external development, testing, and manufacturing partners
  • PMP certification or formal project management training is a plus

Education:

  • Bachelor's degree in mechanical engineering, Biomedical Engineering, or related field. Advanced degree preferred.

Apply